autosomal recessive nonsyndromic deafness 16
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the STRC gene on chromosome 15q15
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autosomal recessive nonsyndromic deafness 16
Summary
autosomal recessive nonsyndromic deafness 16 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 16's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 16's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 16's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 16's subclass of is recorded as autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 16's MeSH descriptor ID is recorded as C566339[6].
- autosomal recessive nonsyndromic deafness 16's OMIM ID is recorded as 603720[7].
- autosomal recessive nonsyndromic deafness 16's Disease Ontology ID is recorded as DOID:0110471[8].
- autosomal recessive nonsyndromic deafness 16's genetic association is recorded as STRC[9].
- autosomal recessive nonsyndromic deafness 16's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110471[10].
- autosomal recessive nonsyndromic deafness 16's exact match is recorded as http://identifiers.org/doid/DOID:0110471[11].
- autosomal recessive nonsyndromic deafness 16's UMLS CUI is recorded as C1863561[12].
- autosomal recessive nonsyndromic deafness 16's ICD-10-CM is recorded as H90.3[13].
- autosomal recessive nonsyndromic deafness 16's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal recessive nonsyndromic deafness 16's Mondo ID is recorded as MONDO_0011364[15].
- autosomal recessive nonsyndromic deafness 16's UniProt disease ID is recorded as DI-00863[16].